CMT2A

MFN2 | 2004

Illustration of a DNA double helix overlaid on nerve cells, with text reading ‘Experts in CMT: CMT Genes and Subtypes Database

CMT2A is caused by autosomal dominant mutations in the MFN2 gene. This gene provides instructions for producing mitofusin-2, a protein crucial for the normal fusion and transport of mitochondria within nerve cells. Mutations in the MFN2 gene disrupt mitochondrial function in peripheral nerves.

The original cause for CMT2A was believed to be associated with the KIF1B gene (published in 1998). However, in 2004, the actual cause, a mutation in the MFN2 gene, was verified. Since then, this subtype has been known by various names, including CMT2A1, CMT2A2, and CMT2A2A. Regardless of which name, they are all CMT2A. ClinGen fully retracted KIF1B’s connection to CMT in 2020. However, some genetic testing companies still include KIF1B on their gene panels. Read the history here.

CMT2A is autosomal dominant, meaning that just one of the gene’s two copies needs a mutation to cause this subtype.

Clinical Features

The age of symptom onset in CMT2A is variable, ranging from early childhood to adulthood. Symptoms typically begin in the lower extremities and progress to involve the upper limbs. An earlier onset is often associated with a more severe disease. Nerve conduction studies usually show normal or only mildly reduced motor conduction velocities, consistent with an axonal form of CMT.

CMT2A symptoms may include:

  • First symptoms typically appear in the lower extremities
  • Variable age of onset, from childhood through adulthood
  • Weakness in the feet and lower legs
  • Muscle atrophy
  • Foot drop
  • A steppage-style walking pattern
  • Reduced sensation, with pain and temperature sensation often more affected than vibration or position sense
  • Reduced or absent reflexes
  • Foot deformities, including high arches and hammertoes (clawed toes)
  • Contractures or scoliosis, particularly in individuals with early-onset disease
  • Rare features such as optic atrophy, hearing loss, tremor, pyramidal signs, or spasticity
  • Approximately 25% may beonly mildly affected, suggesting incomplete/low penetrance
  • Additional symptoms not listed here

Disease Course

CMT2A shows wide variability in severity and progression. Some individuals are mildly affected, while others develop a more severe disease, particularly when symptoms begin early in life. Disease progression is generally slow, and life expectancy is not reduced.

Clinical Basics

Subtype
CMT2A

Classification
CMT2

Subtype Alias
CMT2A1, CMT2A2, CMT2A2A

Neuropathy Type
Axonal

Inheritance Pattern
Autosomal Dominant

Genetic Context

HGNC-Approved Gene Symbol
MFN2

Gene Full Name
Mitofusin 2

HGNC Gene Alias(es)
CPRP1, KIAA0214, MARF

Chromosome
1p36.22

Zygosity of Responsible Variant
Heterozygous

Mitochondrial Involvement
Yes

ClinVar Pathogenic Variants

View CMT2A ClinVar Variants

GeneReviews®

CMT2A GeneReviews®

More Info

Research Opportunity

CMT Natural History Study

Original Discovery Publications

Note:

Correction of (Zhao 2001) KIF1B-associated CMT2A. KIF1B was fully retracted by ClinGen from CMT in 2020.

Publication Title

Mutations in the Mitochondrial GTPase Mitofusin 2 Cause Charcot-Marie-Tooth Neuropathy Type 2A

Authors

Züchner, S., Mersiyanova, I. V., Muglia, M., Bissar-Tadmouri, N., Rochelle, J., Dadali, E. L., Zappia, M., Nelis, E., Patitucci, A., Senderek, J., Parman, Y., Evgrafov, O., Jonghe, P. D., Takahashi, Y., Tsuji, S., Pericak-Vance, M. A., Quattrone, A., Battaloglu, E., Polyakov, A. V., Timmerman, V., Schröder, J.M., Vance, J. M.

Publication Date
April 4, 2004

Note:

Original CMT2A publication. KIF1B was later retracted after MFN2 identified as the culprit gene.

Publication Title

Charcot-Marie-Tooth Disease Type 2A Caused by Mutation in a Microtubule Motor KIF1Bβ

Authors

Zhao, C., Takita, J., Tanaka, Y., Setou, M., Nakagawa, T., Takeda, S., Yang, H. W., Terada, S., Nakata, T., Takei, Y., Saito, M., Tsuji, S., Hayashi, Y., & Hirokawa, N.

Publication Date
June 1, 2001

Updated: February 7, 2026 | By: K. Raymond

The Dorsal Root

More From The Dorsal Root


Close-up of a doctor’s hand holding a prescription pad while a patient’s wrist is wrapped with metal chains.


When Medicine Lost Its Compass

Evidence failed not because it was wrong, but because it was weaponized. I lived the downstream effects of that failure for more than a decade. This is what happens when medicine forgets that data always ends in a human being.


Illustrated graphic showing large ‘404’ numerals with people interacting with data screens and servers, alongside text reading ‘CMT Genetic Testing Error 404: Gene Not Found’ and ‘Examining Why Less Than Half of All Who Have Charcot-Marie-Tooth Disease Are Not Able to Obtain Genetic Confirmation of Their Disease.


Error 404: Gene Not Found

CMT genetic testing often fails to identify the cause of the disease, even when comprehensive panels are used. Here, we discuss why this happens, what genetic tests can and cannot do, and why a negative result still matters.


Illustrated cover graphic showing a split landform with branching directional arrows, two people with question marks above their heads, and the title ‘SORD Deficiency: Decoding This Newly Discovered and Confusing CMT Subtype.


CMT-SORD: What Is This Unique CMT Subtype?

CMT-SORD is a newly discovered CMT subtype driven by toxic sorbitol accumulation. This article explains how "SORD" works, why this subtype is different, and how it led to the fastest-moving therapeutic program in CMT history.